Antibodies as chimeric effector cell receptors against tumor antigens

ABSTRACT

This invention relates to specific antibodies against ganglioside GD3 called MB3.6 and against protein prostate specific membrane antigen (PSMA) called 3D8, 4D4 and 3E11 when prepared as chimeric molecules with signaling molecules of T cells and other effector cells, and the use thereof in the treatment of cancers expressing these antigens.

STATEMENT ON FEDERALLY-SPONSORED R&D

[0001] No federal funds were used in the creation of this invention.

BACKGROUND OF THE INVENTION

[0002] More than 500,000 Americans die each year from cancers that have proven refractory to traditional methods of treatment, for which new strategies are urgently required. Tumor-associated antigens are selected for therapeutic targets based on their high expression on tumor tissue and a lower expression in normal tissues that will plausibly allow selective targeting of tumorous expression of the antigen. Ganglioside GD3 is expressed at high levels on melanoma, small cell lung cancer and other neuroendocrine tumors. Prostate-specific membrane antigen (PSMA) is selectively expressed at high levels in prostate cancer and other tumors. T cells can penetrate virtually every biologic space and have the power to dispose of normal or malignant cells as seen in viral and autoimmune diseases and in the rare spontaneous remissions of cancer. However, T cells are readily tolerant to self or tumor antigens, and “immune surveillance” has manifestly failed in every cancer that is clinically apparent. There is a strong need and value for means to direct T cells against GD3-expressing and PSMA-expressing cancers. This patent describes specific molecules and means to achieve this goal.

BRIEF SUMMARY OF THE INVENTION

[0003] An antibody against GD3 has been prepared called MB3.6. GD3 is expressed at high levels on melanoma and other neuroendocrine tumors, and low levels on normal tissues. Antibodies against PSMA have been prepared called 3D8, 4D4, 3E11. PSMA is expressed principally in prostate tissue, a non-essential organ, and in prostate cancers. It is the goal of this patent to supply the specificities and affinities to patient T cells without regard for their “endogenous” T cell receptor repertoire, directed by antibody-defined recognition to kill malignant cells based on their expression of antigen. This is achieved by preparing chimeric molecules of these specific antibodies with molecules derived from T cells or related effector cell molecules, which will redirect T cells or other effector cells against the tumor cells in a focused anti-tumor immune response by “re-educating” the patient's immune system.

BRIEF DESCRIPTION OF DRAWINGS

[0004]FIG. 1 shows a chimeric antibody-T cell receptor that employs the zeta chain of the TCR. In this example, a single chain Fv (sFv) version of hMN14 is linked by a CD8α hinge to the TCR zeta chain. The CD8α hinge has been further modified to remove the cysteines involved in CD8 dimerization to improve surface expression.

[0005]FIG. 2A shows the near absence of heterodimer molecules when the native CD8α hinge is employed, although it would be predicted to be the dominant species, with a lower net expression of chimeric molecule relative to endogenous zeta chain. FIG. 2B shows the effect of removing the cysteines, which now allows much increased net expression of chimeric molecule when heterodimer can be expressed.

[0006]FIG. 3 shows diagram and DNA sequence of a chimeric sFv IgTCR, including the CD8α hinge modified-to-remove cysteines, within a retroviral vector. This example IgTCR molecule (using hMN14 antibody specific to CEA antigen, not part of this application) occupies nucleotides 2426 to 3766. (The vector sequences are incidental.) Equivalent versions using the antibodies MB3.6, 3D8, 4D4, 3E11 are prepared in analogous manner to create IgTCR, or other Ig-chimeric molecules.

[0007]FIG. 4 shows the DNA sequence of:

[0008] A., B. leader plus VH and leader plus VL that specifies MB3.6.

[0009] C. As example, the VL and leader are joined with linker to VH to create MB3.6 sFv as shown, that is subsequently used in creating chimeric molecules. Other means of generating sFv are possible and included under this claim, as well as other means of creating antibody chimeric molecules under the intent of this invention.

[0010] D., E. leader plus VH and leader plus VL that specifies 3D8 (includes C domain sequences).

[0011] F., G. leader plus VH and leader plus VL that specifies 4D4 (includes C domain sequences).

[0012] H., I. leader plus VH and leader plus VL that specifies 3E11 (includes C domain sequences).

[0013] These sequences are modified to prepare the sFv used in FIG. 1 and FIG. 3, and similarly for other constructs.

[0014]FIG. 5 shows example of the effect of MB3.6 IgTCR-modified T cells in killing GD3-positive tumor cells, but sparing GD3-negative cells. Other examples with 3D8, 4D4, 3E11 would show specific killing against PSMA-positive cells but not against PSMA-negative cells.

[0015]FIG. 6 shows example of the effect of IgTCR (signal 1) using hMN14 antibody chimerics against CEA (not part of this application) on causing sustained CEA+ tumor cell killing when stimulated in conjunction with CD28 (signal 2) stimulation of the gene-modified T cells via B7 antigen expressed in the tumor cells. (A) Signal 1 alone from tumor cells leads to AICD with declining effector cell numbers, that is reversed with signal 1+2. (B) Signal 1 leads to limited duration of tumor killing because of declining T cell numbers. (C) Signal 1+2 leads to sustained tumor killing because of the sustained and expanding T cell numbers. This example justifies design of IgCD28 molecules to modify patient T cells to supply the second signal on contact with antigen that is necessary to suppress effector cell death and achieve sustained killing activity. The intent of this example is the expectation of utility with analogous constructs using the Ig sequences of this application.

[0016]FIG. 7 shows an example of a design for an IgCD28 using MB3.6, 3D8, 4D4, 3E11. This also uses a modified CD8α hinge. Similar designs for other chimeric molecules with these antibodies are envisioned, with or without hinge that is the same or different.

DETAILED DESCRIPTION OF THE INVENTION

[0017] This patent is intended to cover all chimeric molecules created with the specified antibodies (Ig) (MB3.6, 3D8, 4D4, 3E11) (defined by the variable region sequences of FIG. 4) or their derivatives with cell surface molecules which could be used in redirecting and/or activating T cells or other effector cells in the recognition and attack against tumors expressing the antigens recognized by these antibodies. Other specific antibodies which the inventor or his agents obtain with rights will be similarly appended as claims at such future appropriate time. The chimeric molecules of this claim include, but are not limited to, the following molecules: IgTCR (FIGS. 1&3), which has an antibody binding domain from these antibodies fused to one or more chains of the T cell receptor complex; IgCD28 (FIG. 7), which has an antibody binding domain from these antibodies fused to the CD28 T cell co-receptor molecule; IgLFA-1, which has an antibody binding domain from these antibodies fused to the LFA-1 T cell co-receptor/adhesion molecule; IgCD2, which has an antibody binding domain from these specific antibodies fused to the CD2 T cell co-receptor/adhesion molecule; and by analogy, any other T cell or effector cell molecules which are usefully employed in chimeric structures with these antibody binding domains. The chimeric molecules may themselves incorporate cytoplasmic signaling domains, as in the previous examples. Or the chimeric molecules may instead be non-signaling, such as examples of Ig linked to TCR α or β chains, or Ig linked to Fc receptor (FcR) non-signaling chains, that in turn associate with signaling chains to activate cellular functions. These chimeric molecules may additionally incorporate spacer domains or epitope tags. Single-chain Fv (sFv) versions of these antibodies have been favored for use in these constructs, but Fab or other IgG chimeric molecules would be equally included under this invention. The initial description of some of these preparations is contained in Yun et al, 2000. This demonstrates reduction to practice of the concepts contained herein for the MB3.6 antibody, with expectation of similar results for the other antibodies specified in this invention.

[0018] The invention additionally allows for the presence of a (GSGGS)3 linker in the sFv of the Ig portion of the chimeric molecules (e.g., FIG. 4C). Whereas the sFv antibodies may frequently not fold properly to maintain stability, I included the extra serine to improve hydration and sFv folding versus the typical (GGGGS)3 linker that has been associated in some cases with abolished or diminished sFv affinity (e.g., Brinkmann et al, 1993). This strategy with an antibody not covered under this patent (hMN14) led to an sFv virtually indistinguishable from the monovalent binding affinity of the parental antibody (Nolan et al, 1999). Such tests have not been performed with the current antibodies, but all have maintained antigen recognition after sFv modification with this linker.

[0019] The invention additionally allows for the modification-to-remove cysteines in the CD8α hinge domain to improve the surface expression of the chimeric molecules (Nolan et al, 1999). Free cysteines of the hinge of the heterodimer of zeta:sFv-hinge-zeta target this molecular complex for destruction, reducing the net amount of chimeric molecule expression on the cell surface. (The homodimer (sFv-hinge-zeta)₂ has safe pairing of cysteines to spare this specific configuration from destruction. More heterodimer is expected because of binomial considerations where the endogenous zeta exceeds the transduced zeta chimera as is typical.) This principle is demonstrated by the poor expression of heterodimers of such molecules where the cysteine residues are retained (Moritz et al, 1995) and their excellent expression when I modified-to-remove these cysteines (Nolan et al, 1999) (FIG. 2). The efficacy of T cell functions through surface receptors are generally higher with higher surface expression, which the rescue (i.e., non-destruction) of heterodimers would allow. These chimeric molecules are introduced into patient T cells by gene therapy techniques, such as by retroviral vector transduction or other methods. This method of improving cell surface expression is cross-referenced (Junghans Provisional Patent No. 60/250,087).

[0020] In one example, IgTCR (FIG. 1) provides signal 1, which directs T cell killing (e.g., FIG. 5); IgCD28 (FIG. 7) provides signal 2, which suppresses activation induced cell death of T cells and allows sustained proliferation and survival (FIG. 6); and IgLFA1, which provides signal 3 and supports secretion of interleukin 2, an essential T cell growth factor. Combinations of signals can yield improved T cell survival and tumor cell killing (FIG. 6). The invention allows for use of these and/or analogous chimeric molecules of hMN14 alone or in any combination.

[0021] The combination use of such chimeric molecules in treatment of cancers is a further part of the claim. This applies an understanding that more than one signal is required for sustained antitumor efficacy. This application specifically envisions that the same antibody binding domain is applied in the additional chimeric receptor molecules such that encounter with the same tumor antigen successfully triggers more than one signal in the effector cell. Alternatively, additional signaling chimeric molecules may have engineered Ig specificities which direct them to different surface molecules on the tumor cell, rather than to the same one, to avoid binding site competition or to regulate the amount of receptor stimulation where this regulation enhances the desired outcome of antitumor efficacy in therapy.

[0022] The purpose of this invention is to educate immune effector cells to attack GD3-expressing or PSMA-expressing tumor cells. Advantages are that the sequences used to recognize GD3 or PSMA in their conjugation with T cell molecules leads to direct recognition of GD3+ or PSMA+ tumors by human T cells, and hinge and sFv linker modifications make the surface expression more efficient with advantages in anti-tumor activity. Presently, treatments for these cancers are chemotherapy, immunotherapy, surgery and radiation, which are rarely or never curative for metastatic disease. A critical component of this patent for therapy is the specific antibodies that recognize these antigens. No other IgTCR or Ig-T cell molecules has the amino acid sequence of the GD3 or PSMA antibody recognition domains specified herein, and which I have proven to be effective (e.g., FIG. 5). There is no patent of these sequences in chimeric state with T cell or other effector cell molecules, or with the use of a modified hinge structure. This purpose is expanded to other tumor-associated antigens as appropriate to other antibodies as obtained with rights by the inventor or his agents, which will be appended as supplemental claims at such appropriate time.

[0023] An invention exists as to the general chimeric Ig molecules with cell receptor proteins (Capon et al, 1995). This invention is distinguished by the uniqueness of the antibody sequences employed, by the new concept in modification of hinge domains that improves the expression in cells, and by the combination of such chimeric receptor molecules expressed in effector cells which are stimulated in concert specifically by the same tumor antigen or by a different tumor antigen or antigens. The sequences of these antibodies were not previously patented. The claims of the present patent are restricted to the use of these antibodies and sequences in the preparation of these chimeric molecules for the purposes herein described. These claims as pertaining to these sequences do not extend to other potential uses of these antibodies and their derivatives, which are reserved for potential future applications.

1 19 1 7654 DNA Homo sapiens and Mus sp. CDS (2428)..(3759) Chimeric IgTCR sequence contained in retroviral vector. Retroviral vector sequence (non-coding regions) are incidental to the invention. The translated (coding region) is relevant to the invention. (pertinent to Figure 3.) 1 aagcttgcat gcctgcaggt cgactctagg cacataaaga aaaacataac taaccaagct 60 gcagccgaga cagtgaaaag aaccgttaaa acggtttgtt ttaaataaac tgaattattt 120 agagtcattt ctttggtagg aaagtacatt ggcacgtaaa ggagcccaaa gcaatctgtg 180 gaaagcccag gctgggagcc cagcagtttg catcccctcc tggcgtgtac ctaagggttt 240 cttaattgtg tggtttctaa atcttccaga gggtttgtct cattcacttc cacttcggtg 300 cacaatactt ggacgcggat ttactgtctt agcatctatc ggtggccctt cgattgaggc 360 tgaacctgag gcccacttct tcagcttgtt aaggagagca caagcaccag aagaggctga 420 cccggcagac ctgtgggcat ttttaacaag ggcctcctgg gtctgtggga ggcaggctta 480 cataaggtgc aaattagaaa tataaataat aagcccatat caatttgtca tcttttttta 540 agctcaagtt ttgaaagacc ccacctgtag gtttggcaag ctagcttaag taacgccatt 600 ttgcaaggca tggaaaatac ataactgaga atagagaagt tcagatcaag gttaggaaca 660 gagagacagc agaatatggg ccaaacagga tatctgtggt aagcagttcc tgccccgctc 720 agggccaaga acagttggaa caggagaata tgggccaaac aggatatctg tggtaagcag 780 ttcctgcccc ggctcagggc caagaacaga tggtccccag atgcggtccc gccctcagca 840 gtttctagag aaccatcaga tgtttccagg gtgccccaag gacctgaaat gaccctgtgc 900 cttatttgaa ctaaccaatc agttcgcttc tcgcttctgt tcgcgcgctt ctgctccccg 960 agctcaataa aagagcccac aacccctcac tcggcgcgcc agtcctccga tagactgcgt 1020 cgcccgggta cccgtattcc caataaagcc tcttgctgtt tgcatccgaa tcgtggactc 1080 gctgatcctt gggagggtct cctcagattg attgactgcc cacctcgggg gtctttcatt 1140 tggaggttcc accgagattt ggagacccct gcccagggac caccgacccc cccgccggga 1200 ggtaagctgg ccagcaactt atctgtgtct gtccgattgt ctagtgtcta tgactgattt 1260 tatgcgcctg cgtcggtact agttagctaa ctagctctgt atctggcgga cccgtggtgg 1320 aactgacgag ttcggaacac ccggccgcaa ccctgggaga cgtcccaggg acttcggggg 1380 ccgtttttgt ggcccgacct gagtcctaaa atcccgatcg tttaggactc tttggtgcac 1440 cccccttaga ggagggatat gtggttctgg taggagacga gaacctaaaa cagttcccgc 1500 ctccgtctga atttttgctt tcggtttggg accgaagccg cgccgcgcgt cttgtctgct 1560 gcagcatcgt tctgtgttgt ctctgtctga ctgtgtttct gtatttgtct gaaaatatgg 1620 gcccgggcta gactgttacc actcccttaa gtttgacctt aggtcactgg aaagatgtcg 1680 agcggatcgc tcacaaccag tcggtagatg tcaagaagag acgttgggtt accttctgct 1740 ctgcagaatg gccaaccttt aacgtcggat ggccgcgaga cggcaccttt aaccgagacc 1800 tcatcaccca ggttaagatc aaggtctttt cacctggccc gcatggacac ccagaccagg 1860 tcccctacat cgtgacctgg gaagccttgg cttttgaccc ccctccctgg gtcaagccct 1920 ttgtacaccc taagcctccg cctcctcttc ctccatccgc cccgtctctc ccccttgaac 1980 ctcctcgttc gaccccgcct cgatcctccc tttatccagc cctcactcct tctctaggcg 2040 cccccatatg gccatatgag atcttatatg gggcaccccc gccccttgta aacttccctg 2100 accctgacat gacaagagtt actaacagcc cctctctcca agctcactta caggcttcta 2160 cttagtccag cacgaagtct ggagacctct ggcggcagcc taccaagaac aactggaccg 2220 accggtggta cctcaccctt accgagtcgg cgacacagtg tgggtccgcc gacaccagac 2280 taagaaccta gaacctcgct ggaaaggacc ttacacagtc ctgctgacca cccccaccgc 2340 cctcaaagta gacggcatcg cagcttggat acacgccgcc cacgtgaagg ctgccgaccc 2400 cgggggtgga ccatcctcta gactgcc atg gga tgg agc tgt atc atc ctc ttc 2454 Met Gly Trp Ser Cys Ile Ile Leu Phe 1 5 ttg gta gca aca gct aca ggt gtc cac tcc gac atc cag ctg acc cag 2502 Leu Val Ala Thr Ala Thr Gly Val His Ser Asp Ile Gln Leu Thr Gln 10 15 20 25 agc cca agc agc ctg agc gcc agc gtg ggt gac aga gtg acc atc acc 2550 Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr 30 35 40 tgt aag gcc agt cag gat gtg ggt act tct gta gct tgg tac cag cag 2598 Cys Lys Ala Ser Gln Asp Val Gly Thr Ser Val Ala Trp Tyr Gln Gln 45 50 55 aag cca ggt aag gct cca aag ctg ctg atc tac tgg aca tcc acc cgg 2646 Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile Tyr Trp Thr Ser Thr Arg 60 65 70 cac act ggt gtg cca agc aga ttc agc ggt agc ggt agc ggt acc gac 2694 His Thr Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp 75 80 85 ttc acc ttc acc atc agc agc ctc cag cca gag gac atc gcc acc tac 2742 Phe Thr Phe Thr Ile Ser Ser Leu Gln Pro Glu Asp Ile Ala Thr Tyr 90 95 100 105 tac tgc cag caa tat agc ctc tat cgg tcg ttc ggc caa ggg acc aag 2790 Tyr Cys Gln Gln Tyr Ser Leu Tyr Arg Ser Phe Gly Gln Gly Thr Lys 110 115 120 gtg gaa atc aaa cga ggt ggc tca gga tcg ggt gga tcc ggc tct ggt 2838 Val Glu Ile Lys Arg Gly Gly Ser Gly Ser Gly Gly Ser Gly Ser Gly 125 130 135 ggc tca gga tcg gag gtc caa ctg gtg gag agc ggt gga ggt gtt gtg 2886 Gly Ser Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Val Val 140 145 150 caa cct ggc cgg tcc ctg cgc ctg tcc tgc tcc gca tct ggc ttc gat 2934 Gln Pro Gly Arg Ser Leu Arg Leu Ser Cys Ser Ala Ser Gly Phe Asp 155 160 165 ttc acc aca tat tgg atg agt tgg gtg aga cag gca cct gga aaa ggt 2982 Phe Thr Thr Tyr Trp Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly 170 175 180 185 ctt gag tgg att gga gaa att cat cca gat agc agt acg att aac tat 3030 Leu Glu Trp Ile Gly Glu Ile His Pro Asp Ser Ser Thr Ile Asn Tyr 190 195 200 gcg ccg tct cta aag gat aga ttt aca ata tcg cga gac aac gcc aag 3078 Ala Pro Ser Leu Lys Asp Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys 205 210 215 aac aca ttg ttc ctg caa atg gac agc ctg aga ccc gaa gac acc ggg 3126 Asn Thr Leu Phe Leu Gln Met Asp Ser Leu Arg Pro Glu Asp Thr Gly 220 225 230 gtc tat ttt tgt gca agc ctt tac ttc ggc ttc ccc tgg ttt gct tat 3174 Val Tyr Phe Cys Ala Ser Leu Tyr Phe Gly Phe Pro Trp Phe Ala Tyr 235 240 245 tgg ggc caa ggg acc ccg gtc acc gtc tcc agt gct aag ccc acc acg 3222 Trp Gly Gln Gly Thr Pro Val Thr Val Ser Ser Ala Lys Pro Thr Thr 250 255 260 265 acg cca gcg ccg cga cca cca aca ccg gcg ccc acc atc gcg tcg cag 3270 Thr Pro Ala Pro Arg Pro Pro Thr Pro Ala Pro Thr Ile Ala Ser Gln 270 275 280 ccc ctg tcc ctg cgc cca gag gcg gct cgg cca gcg gcg ggg ggc gca 3318 Pro Leu Ser Leu Arg Pro Glu Ala Ala Arg Pro Ala Ala Gly Gly Ala 285 290 295 gtg cac acg agg ggg ctg gac ttc gcc ctg gat ccc aaa ctc tgc tac 3366 Val His Thr Arg Gly Leu Asp Phe Ala Leu Asp Pro Lys Leu Cys Tyr 300 305 310 ctg ctg gat gga atc ctc ttc atc tat ggt gtc att ctc act gcc ttg 3414 Leu Leu Asp Gly Ile Leu Phe Ile Tyr Gly Val Ile Leu Thr Ala Leu 315 320 325 ttc ctg aga gtg aag ttc agc agg agc gca gag ccc ccc gcg tac cag 3462 Phe Leu Arg Val Lys Phe Ser Arg Ser Ala Glu Pro Pro Ala Tyr Gln 330 335 340 345 cag ggc cag aac cag ctc tat aac gag ctc aat cta gga cga aga gag 3510 Gln Gly Gln Asn Gln Leu Tyr Asn Glu Leu Asn Leu Gly Arg Arg Glu 350 355 360 gag tac gat gtt ttg gac aag aga cgt ggc cgg gac cct gag atg ggg 3558 Glu Tyr Asp Val Leu Asp Lys Arg Arg Gly Arg Asp Pro Glu Met Gly 365 370 375 gga aag ccg aga agg aag aac cct cag gaa ggc ctg tac aat gaa ctg 3606 Gly Lys Pro Arg Arg Lys Asn Pro Gln Glu Gly Leu Tyr Asn Glu Leu 380 385 390 cag aaa gat aag atg gcg gag gcc tac agt gag att ggg atg aaa ggc 3654 Gln Lys Asp Lys Met Ala Glu Ala Tyr Ser Glu Ile Gly Met Lys Gly 395 400 405 gag cgc cgg agg ggc aag ggg cac gat ggc ctt tac cag ggt ctc agt 3702 Glu Arg Arg Arg Gly Lys Gly His Asp Gly Leu Tyr Gln Gly Leu Ser 410 415 420 425 aca gcc acc aag gac acc tac gac gcc ctt cac atg cag gcc ctg ccc 3750 Thr Ala Thr Lys Asp Thr Tyr Asp Ala Leu His Met Gln Ala Leu Pro 430 435 440 cct cgc taa ctcgacgcgg ccgcggatcc ggattagtcc aatttgttaa 3799 Pro Arg agacaggata tcagtggtcc aggctctagt tttgactcaa caatatcacc agctgaagcc 3859 tatagagtac gagccataga taaaataaaa gattttattt agtctccaga aaaagggggg 3919 aatgaaagac cccacctgta ggtttggcaa gctagcttaa gtaacgccat tttgcaaggc 3979 atggaaaata cataactgag aatagagaag ttcagatcaa ggttaggaac agagagacag 4039 cagaatatgg gccaaacagg atatctgtgg taagcagttc ctgccccgct cagggccaag 4099 aacagttgga acaggagaat atgggccaaa caggatatct gtggtaagca gttcctgccc 4159 cggctcaggg ccaagaacag atggtcccca gatgcggtcc cgccctcagc agtttctaga 4219 gaaccatcag atgtttccag ggtgccccaa ggacctgaaa tgaccctgtg ccttatttga 4279 actaaccaat cagttcgctt ctcgcttctg ttcgcgcgct tctgctcccc gagctcaata 4339 aaagagccca caacccctca ctcggcgcgc cagtcctccg atagactgcg tcgcccgggt 4399 acccgtgttc tcaataaacc ctcttgcagt tgcatccgac tcgtggtctc gctgttcctt 4459 gggagggtct ctctgagtga ttgactaccc gtcagcgggg tctttcagtt tctcccacct 4519 acacaggtct cactaacatt cctgatgtgc cgcagggact ccgtcagccc ggtttttgtt 4579 tataataaaa tgcaagaaca gtgttccctt caagccagac tacatcctga ctctcggctt 4639 tataaaagaa tgttgaaggg ctctgtggac tatctgccac acgacttttt aagattttta 4699 tgcctcctgg atgagggatt tagtcaatct atcctcgtct attttgctgg cttctccgta 4759 ttttaaattt ctagtttgca ctcccttcct gagagcacgg cgattgcaga gtagttaata 4819 ctctgagggc aggcttctgt gaaaaggttg cctgggctca gtgtgagatt ttgccataaa 4879 aaggggtcct gcccctgtgt acagacagat cggaatctag agtgcatact cagagtcccc 4939 gcggttccgg ggctctgatc tcagggcatc tttgcctaga gatcctctac gccggacgca 4999 tcgtggccgg gtaccgagct cgaattcgta atcatggtca tagctgtttc ctgtgtgaaa 5059 ttgttatccg ctcacaattc cacacaacat acgagccgga agcataaagt gtaaagcctg 5119 gggtgcctaa tgagtgagct aactcacatt aattgcgttg cgctcactgc ccgctttcca 5179 gtcgggaaac ctgtcgtgcc agctgcatta atgaatcggc caacgcgcgg ggagaggcgg 5239 tttgcgtatt gggcgctctt ccgcttcctc gctcactgac tcgctgcgct cggtcgttcg 5299 gctgcggcga gcggtatcag ctcactcaaa ggcggtaata cggttatcca cagaatcagg 5359 ggataacgca ggaaagaaca tgtgagcaaa aggccagcaa aaggccagga accgtaaaaa 5419 ggccgcgttg ctggcgtttt tccataggct ccgcccccct gacgagcatc acaaaaatcg 5479 acgctcaagt cagaggtggc gaaacccgac aggactataa agataccagg cgtttccccc 5539 tggaagctcc ctcgtgcgct ctcctgttcc gaccctgccg cttaccggat acctgtccgc 5599 ctttctccct tcgggaagcg tggcgctttc tcatagctca cgctgtaggt atctcagttc 5659 ggtgtaggtc gttcgctcca agctgggctg tgtgcacgaa ccccccgttc agcccgaccg 5719 ctgcgcctta tccggtaact atcgtcttga gtccaacccg gtaagacacg acttatcgcc 5779 actggcagca gccactggta acaggattag cagagcgagg tatgtaggcg gtgctacaga 5839 gttcttgaag tggtggccta actacggcta cactagaagg acagtatttg gtatctgcgc 5899 tctgctgaag ccagttacct tcggaaaaag agttggtagc tcttgatccg gcaaacaaac 5959 caccgctggt agcggtggtt tttttgtttg caagcagcag attacgcgca gaaaaaaagg 6019 atctcaagaa gatcctttga tcttttctac ggggtctgac gctcagtgga acgaaaactc 6079 acgttaaggg attttggtca tgagattatc aaaaaggatc ttcacctaga tccttttaaa 6139 ttaaaaatga agttttaaat caatctaaag tatatatgag taaacttggt ctgacagtta 6199 ccaatgctta atcagtgagg cacctatctc agcgatctgt ctatttcgtt catccatagt 6259 tgcctgactc cccgtcgtgt agataactac gatacgggag ggcttaccat ctggccccag 6319 tgctgcaatg ataccgcgag acccacgctc accggctcca gatttatcag caataaacca 6379 gccagccgga agggccgagc gcagaagtgg tcctgcaact ttatccgcct ccatccagtc 6439 tattaattgt tgccgggaag ctagagtaag tagttcgcca gttaatagtt tgcgcaacgt 6499 tgttgccatt gctacaggct cgtggtgtca cgctcgtcgt ttggtatggc ttcattcagc 6559 tccggttccc aacgatcaag gcgagttaca tgatccccca tgttgtgcaa aaaagcggtt 6619 agctccttcg gtcctccgat cgttgtcaga agtaagttgg ccgcagtgtt atcactcatg 6679 gttatggcag cactgcataa ttctcttact gtcatgccat ccgtaagatg cttttctgtg 6739 actggtgagt actcaaccaa gtcattctga gaatagtgta tgcggcgacc gagttgctct 6799 tgcccggcgt caatacggga taataccgcg ccacatagca gaactttaaa agtgctcatc 6859 attggaaaac gttcttcggg gcgaaaactc tcaaggatct taccgctgtt gagatccagt 6919 tcgatgtaac ccactcgtgc acccaactga tcttcagcat cttttacttt caccagcgtt 6979 tctgggtgag caaaaacagg aaggcaaaat gccgcaaaaa agggaataag ggcgacacgg 7039 aaatgttgaa tactcatact cttccttttt caatattatt gaagcattta tcagggttat 7099 tgtctcatga gcggatacat atttgaatgt atttagaaaa ataaacaaat aggggttccg 7159 cgcacatttc cccgaaaagt gccacctgac gtctaagaaa ccattattat catgacatta 7219 acctataaaa ataggcgtat cacgaggccc tttcgtctcg cgcgtttcgg tgatgacggt 7279 gaaaacctct gacacatgca gctcccggag acggtcacag cttgtctgta agcggatgcc 7339 gggagcagac aagcccgtca gggcgcgtca gcgggtgttg gcgggtgtcg gggctggctt 7399 aactatgcgg catcagagca gattgtactg agagtgcacc atatgcggtg tgaaataccg 7459 cacagatgcg taaggagaaa ataccgcatc aggcgccatt cgccattcag gctgcgcaac 7519 tgttgggaag ggcgatcggt gcgggcctct tcgctattac gccagctggc gaaaggggga 7579 tgtgctgcaa ggcgattaag ttgggtaacg ccagggtttt cccagtcacg acgttgtaaa 7639 acgacggcca gtgcc 7654 2 443 PRT Homo sapiens and Mus sp. 2 Met Gly Trp Ser Cys Ile Ile Leu Phe Leu Val Ala Thr Ala Thr Gly 1 5 10 15 Val His Ser Asp Ile Gln Leu Thr Gln Ser Pro Ser Ser Leu Ser Ala 20 25 30 Ser Val Gly Asp Arg Val Thr Ile Thr Cys Lys Ala Ser Gln Asp Val 35 40 45 Gly Thr Ser Val Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys 50 55 60 Leu Leu Ile Tyr Trp Thr Ser Thr Arg His Thr Gly Val Pro Ser Arg 65 70 75 80 Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Phe Thr Ile Ser Ser 85 90 95 Leu Gln Pro Glu Asp Ile Ala Thr Tyr Tyr Cys Gln Gln Tyr Ser Leu 100 105 110 Tyr Arg Ser Phe Gly Gln Gly Thr Lys Val Glu Ile Lys Arg Gly Gly 115 120 125 Ser Gly Ser Gly Gly Ser Gly Ser Gly Gly Ser Gly Ser Glu Val Gln 130 135 140 Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg Ser Leu Arg 145 150 155 160 Leu Ser Cys Ser Ala Ser Gly Phe Asp Phe Thr Thr Tyr Trp Met Ser 165 170 175 Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Ile Gly Glu Ile 180 185 190 His Pro Asp Ser Ser Thr Ile Asn Tyr Ala Pro Ser Leu Lys Asp Arg 195 200 205 Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Phe Leu Gln Met 210 215 220 Asp Ser Leu Arg Pro Glu Asp Thr Gly Val Tyr Phe Cys Ala Ser Leu 225 230 235 240 Tyr Phe Gly Phe Pro Trp Phe Ala Tyr Trp Gly Gln Gly Thr Pro Val 245 250 255 Thr Val Ser Ser Ala Lys Pro Thr Thr Thr Pro Ala Pro Arg Pro Pro 260 265 270 Thr Pro Ala Pro Thr Ile Ala Ser Gln Pro Leu Ser Leu Arg Pro Glu 275 280 285 Ala Ala Arg Pro Ala Ala Gly Gly Ala Val His Thr Arg Gly Leu Asp 290 295 300 Phe Ala Leu Asp Pro Lys Leu Cys Tyr Leu Leu Asp Gly Ile Leu Phe 305 310 315 320 Ile Tyr Gly Val Ile Leu Thr Ala Leu Phe Leu Arg Val Lys Phe Ser 325 330 335 Arg Ser Ala Glu Pro Pro Ala Tyr Gln Gln Gly Gln Asn Gln Leu Tyr 340 345 350 Asn Glu Leu Asn Leu Gly Arg Arg Glu Glu Tyr Asp Val Leu Asp Lys 355 360 365 Arg Arg Gly Arg Asp Pro Glu Met Gly Gly Lys Pro Arg Arg Lys Asn 370 375 380 Pro Gln Glu Gly Leu Tyr Asn Glu Leu Gln Lys Asp Lys Met Ala Glu 385 390 395 400 Ala Tyr Ser Glu Ile Gly Met Lys Gly Glu Arg Arg Arg Gly Lys Gly 405 410 415 His Asp Gly Leu Tyr Gln Gly Leu Ser Thr Ala Thr Lys Asp Thr Tyr 420 425 430 Asp Ala Leu His Met Gln Ala Leu Pro Pro Arg 435 440 3 504 DNA Mus sp. CDS (6)..(425) MB3.6 Heavy chain V region, plus leader 3 tcacc atg aac ttc ggg ttc agc ttg att ttc ctt gtc ctt gtt tta aaa 50 Met Asn Phe Gly Phe Ser Leu Ile Phe Leu Val Leu Val Leu Lys 1 5 10 15 ggt gtc cag tgt gaa gtg gtg gtg gtg gag tct ggg gga ggc ttc gtg 98 Gly Val Gln Cys Glu Val Val Val Val Glu Ser Gly Gly Gly Phe Val 20 25 30 aag cct gga ggg tcc ctg aaa ctc tcc tgt gca gcc gct gga ttc act 146 Lys Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ala Gly Phe Thr 35 40 45 ttc agt aga tat gcc atg tct tgg gtt cgc cag act ccg gag aag agg 194 Phe Ser Arg Tyr Ala Met Ser Trp Val Arg Gln Thr Pro Glu Lys Arg 50 55 60 ctg gag tgg gtc gca acc ata agt agt ggt ggt agt cac acc tac tat 242 Leu Glu Trp Val Ala Thr Ile Ser Ser Gly Gly Ser His Thr Tyr Tyr 65 70 75 cca gac agt gtg aag ggg cga ttc acc atc tcc aga gac aat gcc aag 290 Pro Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys 80 85 90 95 aac acc ctg tac ctg caa atg agc agt ctg agg tct gag gac acg gcc 338 Asn Thr Leu Tyr Leu Gln Met Ser Ser Leu Arg Ser Glu Asp Thr Ala 100 105 110 ata tat tac tgt gca aga ccg ggt tac gac agg ggg gcc tgg ttt ttc 386 Ile Tyr Tyr Cys Ala Arg Pro Gly Tyr Asp Arg Gly Ala Trp Phe Phe 115 120 125 gat gtc tgg ggc gca ggg acc acg gtc acc gtc tcc tca ggtaagtgtg 435 Asp Val Trp Gly Ala Gly Thr Thr Val Thr Val Ser Ser 130 135 140 tcagggtttc acaagaggga ctaaagacat gtcagctaat gtgtgactaa tggtaatgtc 495 actaagctt 504 4 140 PRT Mus sp. 4 Met Asn Phe Gly Phe Ser Leu Ile Phe Leu Val Leu Val Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Val Val Val Glu Ser Gly Gly Gly Phe Val Lys 20 25 30 Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ala Gly Phe Thr Phe 35 40 45 Ser Arg Tyr Ala Met Ser Trp Val Arg Gln Thr Pro Glu Lys Arg Leu 50 55 60 Glu Trp Val Ala Thr Ile Ser Ser Gly Gly Ser His Thr Tyr Tyr Pro 65 70 75 80 Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn 85 90 95 Thr Leu Tyr Leu Gln Met Ser Ser Leu Arg Ser Glu Asp Thr Ala Ile 100 105 110 Tyr Tyr Cys Ala Arg Pro Gly Tyr Asp Arg Gly Ala Trp Phe Phe Asp 115 120 125 Val Trp Gly Ala Gly Thr Thr Val Thr Val Ser Ser 130 135 140 5 483 DNA Mus sp. CDS (16)..(399) MB3.6 Light chain V region, plus leader 5 agggaaagct cgaag atg gtt ttc aca cct cag ata ctt gga ctt atg ctt 51 Met Val Phe Thr Pro Gln Ile Leu Gly Leu Met Leu 1 5 10 ttt tgg att tca gcc tcc aga ggt gat att gtg cta act cag tct cca 99 Phe Trp Ile Ser Ala Ser Arg Gly Asp Ile Val Leu Thr Gln Ser Pro 15 20 25 gcc acc ctg tct gtg act cca gga gat agc gtc agt ctt tcc tgc agg 147 Ala Thr Leu Ser Val Thr Pro Gly Asp Ser Val Ser Leu Ser Cys Arg 30 35 40 gcc agc caa att att agc aac aac cta cac tgg tat caa caa aaa tca 195 Ala Ser Gln Ile Ile Ser Asn Asn Leu His Trp Tyr Gln Gln Lys Ser 45 50 55 60 cat gag tct cca agg ctt ctc atc aag tat gct tcc cag tcc atc tct 243 His Glu Ser Pro Arg Leu Leu Ile Lys Tyr Ala Ser Gln Ser Ile Ser 65 70 75 ggg atc ccc tcc agg ttc agt ggc agt gga tca ggg aca gat ttc act 291 Gly Ile Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr 80 85 90 ctc agt atc aac agt gtg gag act gaa gat ttt gga atg tat ttc tgt 339 Leu Ser Ile Asn Ser Val Glu Thr Glu Asp Phe Gly Met Tyr Phe Cys 95 100 105 caa cag agt aac agc tgg cct ctc acg ttc ggc tcg ggg aca aag ctg 387 Gln Gln Ser Asn Ser Trp Pro Leu Thr Phe Gly Ser Gly Thr Lys Leu 110 115 120 gag atc aaa cgg cgtaagtgtg tcagggtttc acaagaggga ctaaagacat 439 Glu Ile Lys Arg 125 gtcagctaat gtgtgactaa tggtaatgtc acttgtcagg atcc 483 6 128 PRT Mus sp. 6 Met Val Phe Thr Pro Gln Ile Leu Gly Leu Met Leu Phe Trp Ile Ser 1 5 10 15 Ala Ser Arg Gly Asp Ile Val Leu Thr Gln Ser Pro Ala Thr Leu Ser 20 25 30 Val Thr Pro Gly Asp Ser Val Ser Leu Ser Cys Arg Ala Ser Gln Ile 35 40 45 Ile Ser Asn Asn Leu His Trp Tyr Gln Gln Lys Ser His Glu Ser Pro 50 55 60 Arg Leu Leu Ile Lys Tyr Ala Ser Gln Ser Ile Ser Gly Ile Pro Ser 65 70 75 80 Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Ser Ile Asn 85 90 95 Ser Val Glu Thr Glu Asp Phe Gly Met Tyr Phe Cys Gln Gln Ser Asn 100 105 110 Ser Trp Pro Leu Thr Phe Gly Ser Gly Thr Lys Leu Glu Ile Lys Arg 115 120 125 7 258 DNA Mus sp. misc_feature (1)..(258) Light chain leader plus sFv of MB3.6 7 gatatcagat ctcagctgtc tagacatatg gttttcacac ctcagatann nnnnnnnnnn 60 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnngggac aaagctggag 120 atcaaaggtg gctcaggatc gggtggagcc ggctctggtg gctcaggatc ggaagtggtg 180 gtggtggagn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnacc 240 acggtcaccg tctccagt 258 8 682 DNA Mus sp. CDS (20)..(418) 3D8 Heavy chain V region, plus leader 8 tgaacacgga cccctcacc atg aac ttc ggg ctc agc ttg att ttc ctt gtc 52 Met Asn Phe Gly Leu Ser Leu Ile Phe Leu Val 1 5 10 ctt gtt tta aaa ggt gtc cag tgt gaa gtg aag gtg gtg gag tct ggg 100 Leu Val Leu Lys Gly Val Gln Cys Glu Val Lys Val Val Glu Ser Gly 15 20 25 gga ggc tta gtg aag cct gga gcg tct ctg aaa ctc tcc tgt gca gcc 148 Gly Gly Leu Val Lys Pro Gly Ala Ser Leu Lys Leu Ser Cys Ala Ala 30 35 40 tct gga ttc act ttc agt aac tat ggc atg tct tgg gtt cgc cag act 196 Ser Gly Phe Thr Phe Ser Asn Tyr Gly Met Ser Trp Val Arg Gln Thr 45 50 55 tca gac aag agg ctg gag tgg gtc gca tcc att agt agt ggt ggt gat 244 Ser Asp Lys Arg Leu Glu Trp Val Ala Ser Ile Ser Ser Gly Gly Asp 60 65 70 75 agc acc ttc tat gca gac aat gta aag ggc cga ttc acc atc tcc aga 292 Ser Thr Phe Tyr Ala Asp Asn Val Lys Gly Arg Phe Thr Ile Ser Arg 80 85 90 gag aat gcc aag aac acc ctg tac ctg caa atg agt agt ctg aag tct 340 Glu Asn Ala Lys Asn Thr Leu Tyr Leu Gln Met Ser Ser Leu Lys Ser 95 100 105 gag gac acg gcc ttg tat tac tgt gca aga gac gat cta ttt aac tgg 388 Glu Asp Thr Ala Leu Tyr Tyr Cys Ala Arg Asp Asp Leu Phe Asn Trp 110 115 120 ggc caa ggc acc act ctc aca gtc tca tca gccaaaacaa cagccccatc 438 Gly Gln Gly Thr Thr Leu Thr Val Ser Ser 125 130 ggtctatcca ctggcccctg tgtgtggaga tacaattggc tcctcggtga ctttaggatg 498 cctggtcaag ggttatttcc ttgagccagt gaccttgacc tggaactctg gatccctgtc 558 cagtggtgtg cacatcttcc cagctgtctt gcagtctgac ctctacaccc tcagcagctc 618 agtgactgta acctcgagca cctggcccag ccagtccatc acttgcaatg tggcccaccc 678 ggca 682 9 133 PRT Mus sp. 9 Met Asn Phe Gly Leu Ser Leu Ile Phe Leu Val Leu Val Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Lys Val Val Glu Ser Gly Gly Gly Leu Val Lys 20 25 30 Pro Gly Ala Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe 35 40 45 Ser Asn Tyr Gly Met Ser Trp Val Arg Gln Thr Ser Asp Lys Arg Leu 50 55 60 Glu Trp Val Ala Ser Ile Ser Ser Gly Gly Asp Ser Thr Phe Tyr Ala 65 70 75 80 Asp Asn Val Lys Gly Arg Phe Thr Ile Ser Arg Glu Asn Ala Lys Asn 85 90 95 Thr Leu Tyr Leu Gln Met Ser Ser Leu Lys Ser Glu Asp Thr Ala Leu 100 105 110 Tyr Tyr Cys Ala Arg Asp Asp Leu Phe Asn Trp Gly Gln Gly Thr Thr 115 120 125 Leu Thr Val Ser Ser 130 10 729 DNA Mus sp. CDS (15)..(410) 3D8 Light chain V region, plus leader 10 ccgttgccgt cgtg atg agt cct gcc cag ttc ctg ttt ctg tta gtg ctc 50 Met Ser Pro Ala Gln Phe Leu Phe Leu Leu Val Leu 1 5 10 tgg att cag gaa acc aac ggt gat gtt gta atg acc cag act cca ctc 98 Trp Ile Gln Glu Thr Asn Gly Asp Val Val Met Thr Gln Thr Pro Leu 15 20 25 act ttg tcg gtt acc att gga caa cca gcc tct atc tct tgc aag tca 146 Thr Leu Ser Val Thr Ile Gly Gln Pro Ala Ser Ile Ser Cys Lys Ser 30 35 40 agt cag agc ctc tta tat agt aat gga aaa acc tat ttg aat tgg tta 194 Ser Gln Ser Leu Leu Tyr Ser Asn Gly Lys Thr Tyr Leu Asn Trp Leu 45 50 55 60 tta cag agg cca ggc cag tct cca aag cgc cta atc tat ctg gtg tct 242 Leu Gln Arg Pro Gly Gln Ser Pro Lys Arg Leu Ile Tyr Leu Val Ser 65 70 75 aaa ctg gac tct gga gtc cct gac agg ttc act ggc agt gga tca gga 290 Lys Leu Asp Ser Gly Val Pro Asp Arg Phe Thr Gly Ser Gly Ser Gly 80 85 90 aca gat ttt aca ctg aaa atc agc aga gtg gag gct gag gat ttg gga 338 Thr Asp Phe Thr Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Leu Gly 95 100 105 gtt tat tac tgc gtg caa ggt aca cat ttt cct cac acg ttc gga ggg 386 Val Tyr Tyr Cys Val Gln Gly Thr His Phe Pro His Thr Phe Gly Gly 110 115 120 ggg acc aag ctg gaa ata aaa cgg gctgatgctg caccaactgt atccatcttc 440 Gly Thr Lys Leu Glu Ile Lys Arg 125 130 ccaccatcca gtgagcagtt aacatctgga ggtgcctcag tcgtgtgctt cttgaacaac 500 ttctacccca aagacatcaa tgtcaagtgg aagattgatg gcagtgaacg acaaaatggc 560 gtcctgaaca gttggactga tcaggacagc aaagacagca cctacagcat gagcagcacc 620 ctcacgttga ccaaggacga gtatgaacga cataacagct atacctgtga ggccactcac 680 aagacatcaa cttcacccat tgtcaagagc ttcaacagga atgagtgtt 729 11 132 PRT Mus sp. 11 Met Ser Pro Ala Gln Phe Leu Phe Leu Leu Val Leu Trp Ile Gln Glu 1 5 10 15 Thr Asn Gly Asp Val Val Met Thr Gln Thr Pro Leu Thr Leu Ser Val 20 25 30 Thr Ile Gly Gln Pro Ala Ser Ile Ser Cys Lys Ser Ser Gln Ser Leu 35 40 45 Leu Tyr Ser Asn Gly Lys Thr Tyr Leu Asn Trp Leu Leu Gln Arg Pro 50 55 60 Gly Gln Ser Pro Lys Arg Leu Ile Tyr Leu Val Ser Lys Leu Asp Ser 65 70 75 80 Gly Val Pro Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr 85 90 95 Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr Tyr Cys 100 105 110 Val Gln Gly Thr His Phe Pro His Thr Phe Gly Gly Gly Thr Lys Leu 115 120 125 Glu Ile Lys Arg 130 12 736 DNA Mus sp. CDS (14)..(430) 4D4 Heavy chain V region, plus leader 12 actgactcta acc atg gga tgg aga tgg atc ttt ctt ttc ctc ctg tca 49 Met Gly Trp Arg Trp Ile Phe Leu Phe Leu Leu Ser 1 5 10 gga act gca ggt gtc cat tgc cag gtt cag ctg cag cag tct gga cct 97 Gly Thr Ala Gly Val His Cys Gln Val Gln Leu Gln Gln Ser Gly Pro 15 20 25 gag ctg gtg aag cct ggg gct tta gtg aag ata tcc tgc aag gct tct 145 Glu Leu Val Lys Pro Gly Ala Leu Val Lys Ile Ser Cys Lys Ala Ser 30 35 40 ggt tac acc ttc aca agc tac gat ata aac tgg gtg aag cag agg cct 193 Gly Tyr Thr Phe Thr Ser Tyr Asp Ile Asn Trp Val Lys Gln Arg Pro 45 50 55 60 gga cag gga ctt gag tgg att gga tgg att tat cct gga gat ggt ggt 241 Gly Gln Gly Leu Glu Trp Ile Gly Trp Ile Tyr Pro Gly Asp Gly Gly 65 70 75 act aat tac aat gag aaa ttc aag ggc aag gcc aca ctg act gca gac 289 Thr Asn Tyr Asn Glu Lys Phe Lys Gly Lys Ala Thr Leu Thr Ala Asp 80 85 90 aaa tcc tcc agc aca gcc tac atg cag ctc agt agc ctg act tct gag 337 Lys Ser Ser Ser Thr Ala Tyr Met Gln Leu Ser Ser Leu Thr Ser Glu 95 100 105 aac tct gca gtc tat ttc tgt gca aga ggg ggt aac ttc cct tct tat 385 Asn Ser Ala Val Tyr Phe Cys Ala Arg Gly Gly Asn Phe Pro Ser Tyr 110 115 120 gct atg gac tac tgg ggt caa gga acc tca gtc acc gtc tcc tca 430 Ala Met Asp Tyr Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ser 125 130 135 gccaaaacga cacccccatc tgtctatcca ctggcccctg gatctgctgc ccaaactaac 490 tccatggtga ccccgggatg cctggtcaag ggctatttcc ctgagccagt gacagtgacc 550 tggaactctg gatccctgtc cagcggtgtg cacaccttcc cagctgtcct gcagtctgac 610 ctctacactc tgagcagctc agtgactgtc ccctccagca cctggcccag cgagaccgtc 670 acctgcaacg ttgcccaccc ggccagcagc accaaggtgg acaagaaaat tgtgcccagg 730 gattgt 736 13 139 PRT Mus sp. 13 Met Gly Trp Arg Trp Ile Phe Leu Phe Leu Leu Ser Gly Thr Ala Gly 1 5 10 15 Val His Cys Gln Val Gln Leu Gln Gln Ser Gly Pro Glu Leu Val Lys 20 25 30 Pro Gly Ala Leu Val Lys Ile Ser Cys Lys Ala Ser Gly Tyr Thr Phe 35 40 45 Thr Ser Tyr Asp Ile Asn Trp Val Lys Gln Arg Pro Gly Gln Gly Leu 50 55 60 Glu Trp Ile Gly Trp Ile Tyr Pro Gly Asp Gly Gly Thr Asn Tyr Asn 65 70 75 80 Glu Lys Phe Lys Gly Lys Ala Thr Leu Thr Ala Asp Lys Ser Ser Ser 85 90 95 Thr Ala Tyr Met Gln Leu Ser Ser Leu Thr Ser Glu Asn Ser Ala Val 100 105 110 Tyr Phe Cys Ala Arg Gly Gly Asn Phe Pro Ser Tyr Ala Met Asp Tyr 115 120 125 Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ser 130 135 14 504 DNA Mus sp. CDS (7)..(402) 4D4 Light chain V region, plus leader 14 ctcaaa atg aag ttg cct gtt agg ctg ttg gtg ctg atg ttc tgg att 48 Met Lys Leu Pro Val Arg Leu Leu Val Leu Met Phe Trp Ile 1 5 10 cct gct tcc aac agt gat gtt ttg atg acc caa tct cca ctc tcc ctg 96 Pro Ala Ser Asn Ser Asp Val Leu Met Thr Gln Ser Pro Leu Ser Leu 15 20 25 30 cct gtc agt ctt gga gat caa gcc tcc atc tct tgc aga tct agt cag 144 Pro Val Ser Leu Gly Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser Gln 35 40 45 agc att gtc cat agt aat gga gac acc tat tta gaa tgg tac ctg cag 192 Ser Ile Val His Ser Asn Gly Asp Thr Tyr Leu Glu Trp Tyr Leu Gln 50 55 60 aaa cca ggc cag tct cca aag ctc ctg atc tac aag gtt tcc gac cga 240 Lys Pro Gly Gln Ser Pro Lys Leu Leu Ile Tyr Lys Val Ser Asp Arg 65 70 75 ttt tct ggg gtc cca gac agg ttc agt ggc agt gga tca ggg aca gat 288 Phe Ser Gly Val Pro Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp 80 85 90 ttc aca ctc aag atc agc aga gtg gag gct gag gat ctg gga gtt tat 336 Phe Thr Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr 95 100 105 110 ttc tgc ttt caa ggt tca cat gtt ccg tac gcg ttc gga ggg ggg acc 384 Phe Cys Phe Gln Gly Ser His Val Pro Tyr Ala Phe Gly Gly Gly Thr 115 120 125 aag ctg gaa ata aaa cgg gctgatgctg caccaactgt atccatcttc 432 Lys Leu Glu Ile Lys Arg 130 ccaccatcca gtgagcagtt aacatctgga ggtgcctcag tcgtgtgctt cttgaacaac 492 ttctacccca aa 504 15 132 PRT Mus sp. 15 Met Lys Leu Pro Val Arg Leu Leu Val Leu Met Phe Trp Ile Pro Ala 1 5 10 15 Ser Asn Ser Asp Val Leu Met Thr Gln Ser Pro Leu Ser Leu Pro Val 20 25 30 Ser Leu Gly Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Ile 35 40 45 Val His Ser Asn Gly Asp Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro 50 55 60 Gly Gln Ser Pro Lys Leu Leu Ile Tyr Lys Val Ser Asp Arg Phe Ser 65 70 75 80 Gly Val Pro Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr 85 90 95 Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr Phe Cys 100 105 110 Phe Gln Gly Ser His Val Pro Tyr Ala Phe Gly Gly Gly Thr Lys Leu 115 120 125 Glu Ile Lys Arg 130 16 761 DNA Mus sp. CDS (62)..(478) 3E11 Heavy chain V region, plus leader 16 cctggattca atttccagtt cctcacattc agtgatcagc actgaacacg gacccctcac 60 c atg aac ttc ggg ctc agc ttg att ttc ctt gtc ctt gtt tta aaa ggt 109 Met Asn Phe Gly Leu Ser Leu Ile Phe Leu Val Leu Val Leu Lys Gly 1 5 10 15 gtc cag tgt gaa gtg aaa ctg gtg gag tct ggg gga gac tta atg aac 157 Val Gln Cys Glu Val Lys Leu Val Glu Ser Gly Gly Asp Leu Met Asn 20 25 30 cct gga gcg tct ctg aaa ctc tcc tgt gca gcc tct gga ttc agt ttc 205 Pro Gly Ala Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Ser Phe 35 40 45 agt aac tat ggc atg tct tgg gtt cgc cag act tca gac aag agg ctg 253 Ser Asn Tyr Gly Met Ser Trp Val Arg Gln Thr Ser Asp Lys Arg Leu 50 55 60 gag tgg gtc gct tcc att agt acg ggt ggt gct aat acc ttc tat cca 301 Glu Trp Val Ala Ser Ile Ser Thr Gly Gly Ala Asn Thr Phe Tyr Pro 65 70 75 80 gac aat gta aag ggc cga ttc acc att tcc aga gag aat gcc aag aac 349 Asp Asn Val Lys Gly Arg Phe Thr Ile Ser Arg Glu Asn Ala Lys Asn 85 90 95 acc cta tac ctg caa atg agt agt ctg aag tct gag gac acg gcc ttg 397 Thr Leu Tyr Leu Gln Met Ser Ser Leu Lys Ser Glu Asp Thr Ala Leu 100 105 110 tat ttc tgt gca aga gat agt cac tcc gta ggt tgt tgg ttt gct acc 445 Tyr Phe Cys Ala Arg Asp Ser His Ser Val Gly Cys Trp Phe Ala Thr 115 120 125 tgg ggc caa ggg act ctg gtc act gtc tct gca gccaaaacaa cacccccatc 498 Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ala 130 135 agtctatcca ctggcccctg ggtgtggaga tactactggt tcctccgtga ctctgggatg 558 cctggtcaag ggctacttcc ctgagtcagt gactgtgact tggaactccg gatccctgcc 618 cagcagtgtg cacaccttcc cagctctcct gcagtctgga ctctacacta tgagcagctc 678 agtgactgtc ccctccagca cctggccaag ccagaccgtt acctgcagtg ttgctcaccc 738 agccagcagc accacggtgg aca 761 17 139 PRT Mus sp. 17 Met Asn Phe Gly Leu Ser Leu Ile Phe Leu Val Leu Val Leu Lys Gly 1 5 10 15 Val Gln Cys Glu Val Lys Leu Val Glu Ser Gly Gly Asp Leu Met Asn 20 25 30 Pro Gly Ala Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Ser Phe 35 40 45 Ser Asn Tyr Gly Met Ser Trp Val Arg Gln Thr Ser Asp Lys Arg Leu 50 55 60 Glu Trp Val Ala Ser Ile Ser Thr Gly Gly Ala Asn Thr Phe Tyr Pro 65 70 75 80 Asp Asn Val Lys Gly Arg Phe Thr Ile Ser Arg Glu Asn Ala Lys Asn 85 90 95 Thr Leu Tyr Leu Gln Met Ser Ser Leu Lys Ser Glu Asp Thr Ala Leu 100 105 110 Tyr Phe Cys Ala Arg Asp Ser His Ser Val Gly Cys Trp Phe Ala Thr 115 120 125 Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ala 130 135 18 698 DNA Mus sp. CDS (6)..(401) 3E11 Light chain V region, plus leader 18 ccagc atg ggc atc aag atg gaa tca cag act ctg gtc ttc ata tcc ata 50 Met Gly Ile Lys Met Glu Ser Gln Thr Leu Val Phe Ile Ser Ile 1 5 10 15 ctg ctc tgg tta tat gga gct gat ggg aac att gta atg acc caa tct 98 Leu Leu Trp Leu Tyr Gly Ala Asp Gly Asn Ile Val Met Thr Gln Ser 20 25 30 ccc aaa tcc atg tcc atg tca gta gga gag agg gtc acc ttg acc tgc 146 Pro Lys Ser Met Ser Met Ser Val Gly Glu Arg Val Thr Leu Thr Cys 35 40 45 aag gcc agt gag aat gtg gtt act tat gtt tcc tgg tat caa cag aaa 194 Lys Ala Ser Glu Asn Val Val Thr Tyr Val Ser Trp Tyr Gln Gln Lys 50 55 60 cca gag cag tct cct aaa ctg ctg ata tac ggg gca tcc aac cgg tac 242 Pro Glu Gln Ser Pro Lys Leu Leu Ile Tyr Gly Ala Ser Asn Arg Tyr 65 70 75 act ggg gtc ccc gat cgc ttc aca ggc agt gga tct gca aca gat ttc 290 Thr Gly Val Pro Asp Arg Phe Thr Gly Ser Gly Ser Ala Thr Asp Phe 80 85 90 95 act ctg acc atc agc agt gtg cag gct gaa gac ctt gca gat tat cac 338 Thr Leu Thr Ile Ser Ser Val Gln Ala Glu Asp Leu Ala Asp Tyr His 100 105 110 tgt gga cag ggt tac agc tat ccg tac acg ttc gga ggg ggg acc aag 386 Cys Gly Gln Gly Tyr Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Thr Lys 115 120 125 ctg gaa ata aaa cgg gctgatgctg caccaactgt atccatcttc ccaccatcca 441 Leu Glu Ile Lys Arg 130 gtgagcagtt aacatctgga ggtgcctcag tcgtgtgctt cttgaacaac ttctacccca 501 aagacatcaa tgtcaagtgg aagattgatg gcagtgaacg acaaaatggc gtcctgaaca 561 gttggactga tcaggacagc aaagacagca cctacagcat gagcagcacc ctcacgttga 621 ccaaggacga gtatgaacga cataacagct atacctgtga ggccactcac aagacatcaa 681 cttcacccat cgtcaag 698 19 132 PRT Mus sp. 19 Met Gly Ile Lys Met Glu Ser Gln Thr Leu Val Phe Ile Ser Ile Leu 1 5 10 15 Leu Trp Leu Tyr Gly Ala Asp Gly Asn Ile Val Met Thr Gln Ser Pro 20 25 30 Lys Ser Met Ser Met Ser Val Gly Glu Arg Val Thr Leu Thr Cys Lys 35 40 45 Ala Ser Glu Asn Val Val Thr Tyr Val Ser Trp Tyr Gln Gln Lys Pro 50 55 60 Glu Gln Ser Pro Lys Leu Leu Ile Tyr Gly Ala Ser Asn Arg Tyr Thr 65 70 75 80 Gly Val Pro Asp Arg Phe Thr Gly Ser Gly Ser Ala Thr Asp Phe Thr 85 90 95 Leu Thr Ile Ser Ser Val Gln Ala Glu Asp Leu Ala Asp Tyr His Cys 100 105 110 Gly Gln Gly Tyr Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Thr Lys Leu 115 120 125 Glu Ile Lys Arg 130 

What is claimed is:
 1. A chimeric molecule comprised of the GD3 binding domain of antibody MB3.6, with variable gene sequences as specified in FIGS. 4A-C, as a single chain antibody with a (GGSGS)3 linker, the zeta signaling chain of the T cell receptor and an intervening CD8α hinge in which the cysteine residues have been mutated.
 2. A chimeric molecule comprised of the PSMA binding domain of antibody 3D8, with variable gene sequences as specified in FIGS. 4D&E, as a single chain antibody with a (GGSGS)3 linker, the zeta signaling chain of the T cell receptor and an intervening CD8α hinge in which the cysteine residues have been mutated.
 3. A chimeric molecule comprised of the PSMA binding domain of antibody 4D4, with variable gene sequences as specified in FIGS. 4F&G, as a single chain antibody with a (GGSGS)3 linker, the zeta signaling chain of the T cell receptor and an intervening CD8α hinge in which the cysteine residues have been mutated.
 4. A chimeric molecule comprised of the PSMA binding domain of antibody 3E11, with variable gene sequences as specified in FIGS. 4H&I, as a single chain antibody with a (GGSGS)3 linker, the zeta signaling chain of the T cell receptor and an intervening CD8α hinge in which the cysteine residues have been mutated.
 5. Molecules of claim 1-4 in which other signaling chains of T cells or other cell types are substituted, or in which a different hinge molecule or no hinge molecule is substituted, or a combination thereof.
 6. Molecules of claim 1-5 in which at least one of the CDRs of the heavy chain and one of the CDRs of the light chain are preserved in a form (e.g., sFv or Fab) that maintains the binding of the antigen, and/or in which the linker is of different composition. For MB3.6, this specification may be met by one CDR of the heavy chain to maintain antigen binding because of the small size of the ganglioside antigen.
 7. Molecules of claim 1-6 which has been modified in DNA or protein sequence but which retains the specificity and action of these molecules.
 8. The use of molecules of claims 1-7 expressed in T cells or NK cells or other effector cells to treat patients with cancers expressing the GD3 (MB3.6 derivatives) or PSMA antigen (3D8, 4D4, 3E11 derivatives).
 9. The combination use of molecules of claims 1-7 expressed in T cells or NK cells or other effector cells to treat patients with cancers expressing the GD3 (MB3.6 derivatives) or PSMA antigen (3D8, 4D4, 3E11 derivatives), together with each other or with heterologous constructs to engage additional stimulatory and functional properties of the effector cells to enhance the antitumor therapeutic efficacy. 